Catalog Number

-

Brand Name

LIFESTYLES

Version/Model Number

8502

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

Yes

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

HIS

Product Code Name

Condom

Public Device Record Key

0dfd0529-e067-4c06-af22-04963699dc1d

Public Version Date

December 21, 2018

Public Version Number

5

DI Record Publish Date

July 11, 2016

Package DI Number

10070907285029

Quantity per Package

4

Contains DI Package

00070907285022

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

inner